Abstract: Disclosed herein are system, method, and computer program product embodiments for accessing a data service using a data service Uniform Resource Identifier (URI) object. An embodiment operates extracting a name-value pair of each parameter stored in the data service class object. The embodiment generates a parameter context URI using the one or more extracted name-value pairs according to a data service specification of the data service. The embodiment extracts one or more filter range items for each filter option stored in the data service class object. The embodiment generates a filter context URI using the one or more extracted filter range items according to the data service specification of the data service. The embodiment generates a context URI using the parameter context URI and the filter context URI. The embodiment then accesses the data service according to the context URI.

Abstract: To print electronic documents from large HTML screens, a user interface component rendered by a computer application on a display device is identified. The user interface component is divided into multiple sub-components. Each sub-component is converted into a respective canvas component resulting in multiple canvas components. A size of each sub-component is selected such that a time taken to convert each sub-component into the respective canvas component is less than a threshold timeout associated with the computer application that rendered the user interface component. The multiple canvas components are converted into a portable document format (PDF) document. The PDF document is displayed on the display device.

Abstract: The present invention provides for novel methods for regulating and detecting the cytosine methylation status of DNA. The invention is based upon identification of a novel and surprising catalytic activity for the family of TET proteins, namely TET1, TET2, TET3, and CXXC4. The novel activity is related to the enzymes being capable of converting the cytosine nucleotide 5-methylcytosine into 5-hydroxymethylcytosine by hydroxylation.

Abstract: Various embodiments for providing a user interface test and validation system are described herein. An embodiment operates by determining user interface (UI) settings and metadata, and fetching data corresponding to the metadata. A plurality of test procedures corresponding to the UI element are identified. A plurality of states to be present in a rendering of the UI element based on the plurality of test procedures, the metadata, and the data are identified. A rendering of the UI element is validated against the plurality of states. A test report is provided based on the validating.

Abstract: The present application provides compounds that are PAPD5 inhibitors and are useful in treating a variety of conditions such as cancer, telomere diseases, and aging-related and other degenerative disorders.

Abstract: The disclosure relates to treating and diagnosing telomere diseases, and methods of screening agents for treating and diagnosing telomere diseases.

Abstract: The present invention provides for methods of epigenetic analysis. In some cases, the methods may include obtaining a sample comprising a nucleic acid sequence. In some cases, the nucleic acid sequence may comprise one or more epigenetic marks. The methods may include performing a sequencing. The methods may include distinguishing a hydroxymethylated base from a methylated base.

Abstract: The disclosure relates to treating and diagnosing telomere diseases, and methods of screening agents for treating and diagnosing telomere diseases.

Abstract: The present invention provides for methods of epigenetic analysis. In some cases, the methods may include obtaining a sample comprising a nucleic acid sequence. In some cases, the nucleic acid sequence may comprise one or more epigenetic marks. The methods may include performing a sequencing. The methods may include distinguishing a hydroxymethylated base from a methylated base.

Abstract: Various embodiments for providing a user interface test and validation system are described herein. An embodiment operates by determining user interface (UI) settings and metadata, and fetching data corresponding to the metadata. A plurality of test procedures corresponding to the UI element are identified. A plurality of states to be present in a rendering of the UI element based on the plurality of test procedures, the metadata, and the data are identified. A rendering of the UI element is validated against the plurality of states. A test report is provided based on the validating.

Abstract: The disclosure relates to compounds that are, e.g., PAP Associated Domain Containing 5 (PAPD5) inhibitors and methods of use thereof.

Abstract: The present invention provides for methods of epigenetic analysis. In some cases, the methods may include obtaining a sample comprising a nucleic acid sequence. In some cases, the nucleic acid sequence may comprise one or more epigenetic marks. The methods may include performing a sequencing. The methods may include distinguishing a hydroxymethylated base from a methylated base.

Abstract: The present invention provides for methods of epigenetic analysis. In some cases, the methods may include obtaining a sample comprising a nucleic acid sequence. In some cases, the nucleic acid sequence may comprise one or more epigenetic marks. The methods may include performing a sequencing. The methods may include distinguishing a hydroxymethylated base from a methylated base.

Abstract: The present invention provides for novel methods for regulating and detecting the cytosine methylation status of DNA. The invention is based upon identification of a novel and surprising catalytic activity for the family of TET proteins, namely TET1, TET2, TET3, and CXXC4. The novel activity is related to the enzymes being capable of converting the cytosine nucleotide 5-methylcytosine into 5-hydroxymethylcytosine by hydroxylation.

Abstract: The disclosure relates to compounds that are, e.g., PAP Associated Domain Containing 5 (PAPD5) inhibitors and methods of use thereof.

Abstract: The present invention provides methods for performing an imaging method to detect a moiety associated with labeled hydroxymethylated bases in nucleic acid sequences, such as detecting a moiety associated with glucosylated 5-hydroxmethylated cytosines.

Abstract: The present invention provides for novel methods for regulating and detecting the cytosine methylation status of DNA. The invention is based upon identification of a novel and surprising catalytic activity for the family of TET proteins, namely TET1, TET2, TET3, and CXXC4. The novel activity is related to the enzymes being capable of converting the cytosine nucleotide 5-methylcytosine into 5-hydroxymethylcytosine by hydroxylation.

Abstract: Provided herein are methods and kits for distinguishing 5-hydroxymethylcytosine from 5-methylcytosine.

Abstract: The present invention provides for novel methods for regulating and detecting the cytosine methylation status of DNA. The invention is based upon identification of a novel and surprising catalytic activity for the family of TET proteins, namely TET1, TET2, TET3, and CXXC4. The novel activity is related to the enzymes being capable of converting the cytosine nucleotide 5-methylcytosine into 5-hydroxymethylcytosine by hydroxylation.

Abstract: The present invention provides for novel methods for regulating and detecting the cytosine methylation status of DNA. The invention is based upon identification of a novel and surprising catalytic activity for the family of TET proteins, namely TET1, TET2, TET3, and CXXC4. The novel activity is related to the enzymes being capable of converting the cytosine nucleotide 5-methylcytosine into 5-hydroxymethylcytosine by hydroxylation.